Metabolic and structural changes in the myocardium of rats with hypercholesterolemia after prolonged administration of simvastatin

E. S. Belousova, Z. I. Mikashinowich, E. Vinogradova
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Abstract

BACKGROUND: The use of statins in cardiovascular pathologies in some cases is associated with the risk of developing statin-induced myopathy, the mechanisms of which are not fully understood. Only a few studies of molecular changes in the myocardium in statin myopathy are presented in the literature. However, the myocardium, as a type of muscle tissue, can also be involved in the pathological process. In this regard, in our opinion, it is advisable to analyze the biochemical changes in the rat myocardium against the background of the use of simvastatin. AIM: To analysis of the dynamics of changes in the end products of glycolysis and the isoform composition of the giant protein titin in the heart muscle in animals with experimental hypercholesterolemia on the background of long-term administration of simvastatin. MATERIALS AND METHODS: The study was carried out on outbred male rats divided into 3 groups: control group (35 individuals) intact animals; comparison group (35 animals) intact animals treated with simvastatin for two months; experimental group divided into: subgroup 1 (35 individuals) animals with induced alimentary hypercholesterolemia, subgroup 2 (35 individuals) animals with induced alimentary hypercholesterolemia, which were administered simvastatin for two months. During the experiment, the content of the giant sarcomere protein titin, as well as changes in the concentration of pyruvate and lactic acid in the myocardium of the animals of the studied groups were studied. RESULTS: In animals with a physiological course of metabolic processes, the administration of simvastatin caused the accumulation of lactic acid in the myocardium. Under conditions of alimentary hypercholesterolemia under the influence of simvastatin, a decrease in the elevated level of pyruvate and lactic acid was revealed, which is obviously due to a decrease in pathobiochemical shifts in energy metabolism. The determination of the isoform composition of titin made it possible to establish that the administration of simvastatin under conditions of alimentary hypercholesterolemia contributed to the appearance of early dystrophic changes in the myocardium, which is consistent with the results of earlier studies of impaired myocardial contractile activity under the influence of statins. CONCLUSIONS: The results obtained indicate the need for a more thorough study of statins in terms of their safe use in patients with cardiovascular pathology.
长期服用辛伐他汀对高胆固醇血症大鼠心肌代谢和结构的影响
背景:在某些情况下,他汀类药物用于心血管疾病与发生他汀类药物诱导的肌病的风险相关,其机制尚不完全清楚。文献中只有少数关于他汀类药物肌病中心肌分子变化的研究。然而,心肌作为一种肌肉组织,也可以参与病理过程。因此,我们认为,在使用辛伐他汀的背景下,分析大鼠心肌的生化变化是可取的。目的:分析长期服用辛伐他汀对实验性高胆固醇血症动物心肌糖酵解终产物及巨蛋白titin亚型组成的影响。材料与方法:选用远交系雄性大鼠,分为3组:对照组(35只)完整动物;对照组(35只)完整动物,辛伐他汀治疗2个月;实验组分为:诱导性消化道高胆固醇血症亚组1(35只),诱导性消化道高胆固醇血症亚组2(35只),给予辛伐他汀治疗2个月。在实验过程中,研究各组动物心肌巨肌节蛋白titin的含量,以及丙酮酸和乳酸浓度的变化。结果:在有生理代谢过程的动物中,辛伐他汀可引起心肌乳酸的积累。在辛伐他汀影响下的消化道高胆固醇血症条件下,丙酮酸和乳酸的升高水平有所下降,这显然是由于能量代谢的病理生化转变减少所致。通过对他汀同种异构体组成的测定,可以确定在消化性高胆固醇血症条件下服用辛伐他汀会导致心肌出现早期营养不良变化,这与早期他汀类药物影响下心肌收缩活动受损的研究结果一致。结论:所获得的结果表明,需要对他汀类药物在心血管疾病患者中的安全性进行更深入的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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